Explore the Potential with AI-Driven Innovation
This extensive focused library is tailor-made using the latest virtual screening and parameter assessment technology, operated by the Receptor.AI drug discovery platform. This technique is more effective than traditional methods, offering compounds with improved activity, selectivity, and safety.
Our selection of compounds is from a large virtual library of over 60 billion molecules. The production and distribution of these compounds are managed by our partner Reaxense.
In the library, a selection of top modulators is provided, each marked with 38 ADME-Tox and 32 parameters related to physicochemical properties and drug-likeness. Also, every compound comes with its best docking poses, affinity scores, and activity scores, providing a comprehensive overview.
Our high-tech, dedicated method is applied to construct targeted libraries.
Fig. 1. The sreening workflow of Receptor.AI
Our strategy employs molecular simulations to explore an extensive range of proteins, capturing their dynamics both individually and within complexes with other proteins. Through ensemble virtual screening, we address proteins' conformational mobility, uncovering key binding sites at both functional regions and remote allosteric locations. This comprehensive investigation ensures a thorough assessment of all potential mechanisms of action, with the goal of discovering innovative therapeutic targets and lead molecules across across diverse biological functions.
Key features that set our library apart include:
partner
Reaxense
upacc
Q8IZI9
UPID:
IFNL3_HUMAN
Alternative names:
Cytokine Zcyto22; Interleukin-28B; Interleukin-28C
Alternative UPACC:
Q8IZI9; A2BDE1; Q6VN56; Q7Z4J3; Q8IWL6
Background:
Interferon lambda-3, known alternatively as Cytokine Zcyto22, Interleukin-28B, and Interleukin-28C, is a pivotal cytokine with antiviral, antitumour, and immunomodulatory activities. It plays a critical role in the antiviral host defense, especially in epithelial tissues, by acting as a ligand for the IL10RB and IFNLR1 receptor complex. This engagement activates the JAK/STAT signaling pathway, leading to the expression of IFN-stimulated genes (ISG) that mediate the antiviral state.
Therapeutic significance:
Understanding the role of Interferon lambda-3 could open doors to potential therapeutic strategies, particularly in enhancing antiviral and antitumor immunity and modulating immune responses.